Dronabinol
- Product NDC
- 0904-6598
- 11-digit product format
- 009046598
- Labeler code
- 0904
- Product ID
- 0904-6598_255a2c61-0602-4427-9515-2e39bb22575f
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Dronabinol
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- Major Pharmaceuticals
- Application
- ANDA078292
- Marketing category
- ANDA
- Marketing start
- 2008-06-27
- Marketing end
- 0000-00-00
- Substance
- DRONABINOL
- Active strength
- 5 mg/1
- Pharmacologic classes
- Cannabinoid [EPC],Cannabinoids [CS]
- DEA schedule
- CIII
- NDC exclude flag
- No
- Listing certified through
- 2019-12-31
- Current FDA listing
- Historical FDA.report record